公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2014 | Reevesioside A, a cardenolide glycoside, induces anticancer activity against human hormone-refractory prostate cancers through suppression of c-myc expression and induction of G1 arrest of the cell cycle | Leu W.-J.; Chang H.-S.; Chan S.-H.; Hsu J.-L.; Yu C.-C.; LIH-CHING HSU ; Chen I.-S.; JIH-HWA GUH | PLoS ONE | 26 | 24 | |
2013 | Reevesioside F induces potent and efficient anti-proliferative and apoptotic activities through Na+/K+-ATPase α3 subunit-involved mitochondrial stress and amplification of caspase cascades | Chan S.-H.; Leu W.-J.; LIH-CHING HSU ; Chang H.-S.; Hwang T.-L.; Chen I.-S.; Chen C.-S.; JIH-HWA GUH | Biochemical Pharmacology | 17 | 15 | |
2015 | Repurposing of nitroxoline as a potential anticancer agent against human prostate cancer - A crucial role on AMPK/mTOR signaling pathway and the interplay with Chk2 activation | Chang W.-L.; LIH-CHING HSU ; Leu W.-J.; Chen C.-S.; JIH-HWA GUH | Oncotarget | 39 | 35 | |
2015 | Repurposing of phentolamine as a potential anticancer agent against human castration-resistant prostate cancer: A central role on microtubule stabilization and mitochondrial apoptosis pathway | Ho C.-H.; Hsu J.-L.; SHIH-PING LIU ; LIH-CHING HSU ; Chang W.-L.; Chao C.C.-K.; JIH-HWA GUH | Prostate | 14 | 14 | |
2018 | Retraction of "Development of Novel Adenosine Monophosphate-Activated Protein Kinase Activators" | JIH-HWA GUH ; Chang, Wei-Ling; Yang, Jian; Lee, Su-Lin; Wei, Shuo; Wang, Dasheng; Kulp, Samuel K; Chen, Ching-Shih | Journal of medicinal chemistry | | | |
1998 | Retraction: Mechanism of anti-proliferation caused by YC-1, an indazole derivative, in cultured rat A10 vascular smooth-muscle cells (Biochemical Journal (1995) 306 (787-792)) | Cheng, Zhijiao; JIH-HWA GUH ; Lee, Fangyu; Kuo, Shengchen | Biochemical Journal | | | |
2015 | Ring fusion strategy for synthesis and lead optimization of sulfur-substituted anthra[1,2-c[[1,2,5]thiadiazole-6,11-dione derivatives as promising scaffold of antitumor agents | Lee Y.-R.; Chen T.-C.; Lee C.-C.; Chen C.-L.; Ahmed Ali A.A.; Tikhomirov A.; JIH-HWA GUH ; Yu D.-S.; Huang H.-S. | European Journal of Medicinal Chemistry | 25 | 23 | |
2014 | Ring fusion strategy for the synthesis of anthra[2,3-d ]oxazole-2-thione-5,10-dione homologues as DNA topoisomerase inhibitors and as antitumor agents | Chen C.-L.; Liu F.-L.; Lee C.-C.; Chen T.-C.; Chang W.-W.; JIH-HWA GUH ; Ahmed Ali A.A.; Chang D.-M.; Huang H.-S. | European Journal of Medicinal Chemistry | 20 | 17 | |
2012 | Rottlerin potentiates camptothecin-induced cytotoxicity in human hormone refractory prostate cancers through increased formation and stabilization of topoisomerase I-DNA cleavage complexes in a PKCδ-independent pathway | Hsu J.-L.; Ho Y.-F.; TSAI-KUN LI ; Chen C.-S.; LIH-CHING HSU ; JIH-HWA GUH | Biochemical Pharmacology | 18 | 16 | |
2018 | Ruthenium (II) complexes containing dehydroacetic acid and its imine derivative ligands. Synthesis, characterization and cancer cell growth anti-proliferation activity (GI50) study | Chen K.-H.; Lin T.-H.; Hsu T.-E.; Li Y.-J.; Chen G.-H.; Leu W.-J.; JIH-HWA GUH ; Lin C.-H.; Huang J.-H. | Journal of Organometallic Chemistry | 8 | 6 | |
2015 | Structural studies and anticancer activity of a novel class of β-peptides | Kudryavtsev K.V.; Yu C.-C.; Ivantcova P.M.; Polshakov V.I.; Churakov A.V.; Br?se S.; Zefirov N.S.; JIH-HWA GUH | Chemistry - An Asian Journal | 15 | 14 | |
2024 | Structure-based design, synthesis and biological evaluation of N-substituted 6H-thiochromeno[2,3–c]quinolin-12(12H)-one as potential breast cancer drugs | Sumitra, Maryam Rachmawati; Chen, Lung Ching; Tsai, Wei Chen; Ansar, Muhamad; Lawal, Bashir; Mokgautsi, Ntlotlang; JIH-HWA GUH ; Wu, Alexander T.H.; Huang, Hsu Shan | Arabian Journal of Chemistry | | | |
2013 | Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology | Chen C.-L.; Chang D.-M.; Chen T.-C.; Lee C.-C.; Hsieh H.-H.; Huang F.-C.; Huang K.-F.; JIH-HWA GUH ; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 35 | 34 | |
2014 | Synthesis and anti-cancer activity of a glycosyl library of \varvec{N} N -acetylglucosamine-bearing oleanolic acid | Zeng, Yi-Bing; Hsiao, Hsin-Min; Chan, She-Hung; Wang, Ying-Hsin; Lin, You-Yu; Kuo, Yu-Hsuan; JIH-HWA GUH ; PI-HUI LIANG | Molecular Diversity | 14 | | |
2019 | Synthesis and biological evaluation of anthra[1,9-cd]pyrazol-6(2H)-one scaffold derivatives as potential anticancer agents | Chen T.-C.; JIH-HWA GUH ; Hsu H.-W.; Chen C.-L.; Lee C.-C.; Wu C.-L.; Lee Y.-R.; JING-JER LIN ; Yu D.-S.; Huang H.-S. | Arabian Journal of Chemistry | 8 | 7 | |
2016 | Synthesis and characterization of ruthenium compounds incorporating keto-amine ligands. The applications of catalytic transfer hydrogenation and cancer cell inhibition | Lin T.-H.; Das K.; Datta A.; Leu W.-J.; Hsiao H.-C.; Lin C.-H.; JIH-HWA GUH ; Huang J.-H. | Journal of Organometallic Chemistry | 8 | 8 | |
2011 | Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors | Huang W.-J.; CHING-CHOW CHEN ; Chao S.-W.; Yu C.-C.; Yang C.-Y.; JIH-HWA GUH ; Lin Y.-C.; Kuo C.-I.; Yang P.; Chang C.-I. | European Journal of Medicinal Chemistry | 37 | 35 | |
2013 | Synthesis of a chlorogenin glycoside library using an orthogonal protecting group strategy | Wang Y.-H.; Yeh H.-W.; Wang H.-W.; Yu C.-C.; JIH-HWA GUH ; Liu D.-Z.; PI-HUI LIANG | Carbohydrate Research | 13 | 13 | |
2012 | Synthesis, antiproliferative activities and telomerase inhibition evaluation of novel asymmetrical 1,2-disubstituted amidoanthraquinone derivatives | Lee C.-C.; Huang K.-F.; Lin P.-Y.; Huang F.-C.; Chen C.-L.; Chen T.-C.; JIH-HWA GUH ; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 27 | 23 | |
2018 | Synthesis, characterization and cancer cell growth inhibition activity of ruthenium(II) complexes bearing bidentate pyrrole-imine ligands | Chen G.-H.; Leu W.-J.; JIH-HWA GUH ; Lin C.-H.; Huang J.-H. | Journal of Organometallic Chemistry | 7 | 5 | |